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[ CAS No. 1137576-38-5 ] {[proInfo.proName]}

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Chemical Structure| 1137576-38-5
Chemical Structure| 1137576-38-5
Structure of 1137576-38-5 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1137576-38-5 ]

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Product Details of [ 1137576-38-5 ]

CAS No. :1137576-38-5 MDL No. :MFCD18072689
Formula : C4HCl2IN2 Boiling Point : -
Linear Structure Formula :- InChI Key :YKSZLCOPANWXES-UHFFFAOYSA-N
M.W : 274.87 Pubchem ID :56763824
Synonyms :

Calculated chemistry of [ 1137576-38-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 44.77
TPSA : 25.78 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.0 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.88
Log Po/w (XLOGP3) : 2.78
Log Po/w (WLOGP) : 2.39
Log Po/w (MLOGP) : 1.76
Log Po/w (SILICOS-IT) : 3.32
Consensus Log Po/w : 2.43

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -3.79
Solubility : 0.0447 mg/ml ; 0.000163 mol/l
Class : Soluble
Log S (Ali) : -2.98
Solubility : 0.29 mg/ml ; 0.00105 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.83
Solubility : 0.0403 mg/ml ; 0.000147 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.9

Safety of [ 1137576-38-5 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1137576-38-5 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1137576-38-5 ]

[ 1137576-38-5 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 1193-21-1 ]
  • [ 1137576-38-5 ]
YieldReaction ConditionsOperation in experiment
83% Synthesis of 4,6-dichloro-5-iodo-pyrimidine (8a): 4,6-Dichloropyrimidine 6 (149 mg, 1.0 mmol) in THF (2 mL) was added to a solution of TMPZnCl.LiCl (2) (1.3 M in THF, 0.85 mL, 1.1 mmol) at 25 C. and the reaction mixture was then stirred at this temperature for 45 min according to TP 2. I2 (381 mg, 1.5 mmol) dissolved in dry THF (2 mL) was then dropwise added and the resulting mixture was stirred for 0.5 h. The reaction mixture was quenched with a sat. aq. Na2S2O3 solution (10 mL) and with a sat. aq. NH4Cl solution (20 mL), extracted with diethyl ether (3×50 mL) and driedanhydrous Na2SO4. After filtration, the solvent was evaporated in vacuo. Purification by flash-chromatography (CH2Cl2/n-pentane, 1:4) furnished compound 8a (227 mg, 83%) as a colourless solid.m.p.: 134.9-136.5 C.1H NMR (300 MHz, CDCl3) delta: 8.65 (s, 1 H).13C NMR (75 MHz, CDCl3) delta: 166.6, 156.8, 98.9.MS (70 eV, El) m/z (%): 274 (100) [M+], 239 (27), 97 (12), 83 (12), 57 (21).IR (ATR) v (cm-1): 2923, 2855, 1900, 1499, 1386, 11341, 1296, 1214, 1080, 1014, 790, 763, 745.HRMS (El) for C4HCl2IN2 (273.8561): 273.8565.
  • 2
  • [ 1137576-38-5 ]
  • [ 1137576-39-6 ]
  • 3
  • [ 1137576-38-5 ]
  • [ 106-95-6 ]
  • [ 1137576-40-9 ]
  • 4
  • [ 1137576-38-5 ]
  • [ 1259224-00-4 ]
  • [ 1439395-38-6 ]
YieldReaction ConditionsOperation in experiment
50% With triethylamine; In 1,4-dioxane; at 80℃;Inert atmosphere; To the solution of <strong>[1137576-38-5]4,6-dichloro-5-iodopyrimidine</strong> (5.50 g, 20.00 mmol) (prepared according to the ref of Organic Letters; English; 11; 8; 2009; 1837 - 1840; ) in dioxane (100 mL) was slowly added the solution of tert-butyl l-(4-aminophenyl)cyclobutylcarbamate (5.2 g, 20.00 mmol) in dioxane (20 mL) and Et3N(5 ml). The reaction mixture was stirred at 80C for overnight, lc-ms indicated <strong>[1137576-38-5]4,6-dichloro-5-iodopyrimidine</strong> was completed consumed. After removed the excess solvents under the reduced pressure to get a residue, which was dissolved in Ethyl acetate (250 mL) and washed water and brine. The combined organic layer was dried over Na2S04 and then filtered, the filtrate was concentrated to give the crude product, which was further purified by flash chromatography to afford tert-butyl l-(4-(6-chloro-5-iodopyrimidin-4- ylamino)phenyl)cyclobutylcarbamate. (5.00 g 50% yield).LC/MS: (ESI+): 501 [M+l], 523 [M+Na].
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